Respiratory infections regulated blood cells IFN-β-PD-L1 pathway in pediatric asthma

被引:4
作者
Koelle, Julia [1 ]
Haag, Patricia [1 ]
Vuorinen, Tytti [2 ]
Alexander, Kiefer [3 ]
Rauh, Manfred [3 ]
Zimmermann, Theodor [3 ]
Papadopoulos, Nikolaos G. [4 ,5 ]
Finotto, Susetta [1 ]
机构
[1] Friedrich Alexander Univ FAU Erlangen Nurnberg, Dept Mol Pneumol, Univ Klinikum Erlangen, Erlangen, Germany
[2] Univ Turku, Dept Virol, Turku, Finland
[3] Friedrich Alexander Univ FAU Erlangen Nurnberg, Dept Allergy & Pneumol, Childrens Hosp, Univ Klinikum Erlangen, Erlangen, Germany
[4] Natl & Kapodistrian Univ Athens, Allergy & Clin Immunol Unit, Pediat Clin 2, Athens, Greece
[5] Univ Manchester, Div Infect Immun & Resp Med, Manchester, Lancs, England
关键词
human rhinovirus; IFN beta; PD-L1; pediatric asthma; IFN-GAMMA;
D O I
10.1002/iid3.307
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Respiratory infections, in general, and rhinovirus infection specifically are the main reason for asthma exacerbation in children and programmed cell death protein 1 ligand (PD-L1) expression inhibits T cell responses. Objective Could the interferon (IFN) type I expression in peripheral blood mononuclear cells (PBMCs) improve disease exacerbation in pediatric asthma? Results Here we found increased level of PD-L1 messenger RNA (mRNA) in total blood cells isolated from preschool children with virus-induced asthma, with lower percentage of forced expiratory volume in 1 second and with high serum levels of the C-reactive-protein. Conclusions and Clinical Relevance These data indicate that, in the presence of infection in the airways of preschool children, worse asthma is associated with induced PD-L1 mRNA expression in blood cells. Further, type I IFN, IFN-beta, a cytokine that is involved in the clearance of infections, was found to be associated with a better lung function in asthmatic children. These data suggest that improving peripheral blood IFN type I expression in PBMCs in pediatric asthma could improve disease exacerbation due to suppressing PD-L1 expression in blood cells.
引用
收藏
页码:310 / 319
页数:10
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